Modified Gram-Negative Bacteria For Use As Vaccines

ABSTRACT

The invention relates to Gram-negative bacteria carrying an inactivated gene encoding a glycosyltransferase involved in the synthesis of the core of the LPS of said Gram-negative bacteria, wherein said inactivated gene results in the synthesis of a LPS having a modified core. These strains have an attenuated virulence but induce a humoral immunity sufficient for ensuring vaccination of the host.

FIELD OF THE INVENTION

The invention generally relates to the field of modified gram-negative bacteria for use as vaccines.

BACKGROUND OF THE INVENTION

Gram-negative bacteria are those bacteria that do not retain crystal violet dye in the Gram staining protocol. Many species of Gram-negative bacteria are pathogenic, meaning that they can cause disease in a host organism. This pathogenic capability is usually associated with certain components of Gram-negative cell walls, in particular the lipopolysaccharide (also known as LPS or endotoxin) layer.

LPS is a major component of the outer membrane of Gram-negative bacteria, contributing greatly to the structural integrity of the bacteria, and protecting the membrane from certain kinds of chemical attack. LPS also increases the negative charge of the cell membrane and helps stabilize the overall membrane structure. LPS is an endotoxin, and induces a strong response from normal animal immune systems. LPS is additionally an exogenous pyrogen (external fever-inducing compound). LPS comprises three parts: polysaccharide (O) side chains, a core polysaccharide and lipid A.

Lipid A contains unusual fatty acids (e.g. hydroxy-myristic acid) and is embedded in the outer membrane while the rest of the LPS projects from the surface. Lipid A is a disaccharide with multiple fatty acid tails reaching into the membrane. When bacterial cells are lysed by the immune system, fragments of membrane containing lipid A are released into the circulation, causing fever, diarrhea, and possible fatal endotoxic shock (also called septic shock).

The polysaccharide side chain is referred to as the O-antigen of the bacteria. O side chain (O-antigen) is a polysaccharide chain that extends from the core polysaccharide. The composition of the O side chain varies between different Gram-negative bacterial strains. O side chains are easily recognized by the antibodies of the host, however, the nature of the chain can easily be modified by Gram-negative bacteria to avoid detection.

The core oligosaccharide contains unusual sugars (e.g. KDO, keto-deoxyoctulosonate and heptose), but little is known concerning its role. In particular, its role in virulence has never been studied directly.

Numerous LPS mutants inducing humoral immunity to lipopolysaccharide (LPS) have been proposed as potential vaccines. However, pure LPS mutants or bacteria expressing LPS mutants are generally considered too toxic to be used as vaccines, in particular in view of their strong adverse effects, and there is thus a need for new vaccines, presenting an attenuated virulence and inducing a sufficient humoral immunity for ensuring vaccination of the host.

SUMMARY OF THE INVENTION

The inventors have found that, by modifying a particular structure of the core of the LPS of Gram-negative bacteria, it is possible to obtain strains having an attenuated virulence but inducing a humoral immunity sufficient for ensuring vaccination of the host. Indeed, the inventors have discovered that particular glycosyltransferases involved in the synthesis of the core of the LPS have a critical role in Gram-negative bacteria virulence. When at least one of these glycosyltransferases is inactivated, the modified LPS synthesized by the Gram-negative bacteria induce a strong immune response of the host and its vaccination. Moreover, the inventors have further shown that the administration to a host of a LPS produced by Gram-negative bacteria wherein at least one of said glycosyltransferases is inactivated induces an unspecific immune response and can thus be used as an adjuvant for stimulating the immune system.

DETAILED DESCRIPTION OF THE INVENTION

An object of the invention concerns a Gram-negative bacterium carrying an inactivated gene encoding a glycosyltransferase involved in the synthesis of the core of the LPS of said Gram-negative bacterium,

wherein said glycosyltransferase is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:1 or SEQ ID NO:21, or homologues thereof having an amino acid sequence having at least 50%, particularly at least 60%, more particularly at least 70%, most particularly at least 80% of identity with SEQ ID NO:1 or SEQ ID NO:21, and wherein said inactivated gene encoding a glycosyltransferase involved in the synthesis of the core of the LPS of said Gram-negative bacterium results in the synthesis of a LPS having a modified core.

The inventors have shown that the glycosyltransferase having the amino acid sequence of SEQ ID NO:1 is a glycosyltransferase involved in the synthesis of a particular branched structure of the core of the LPS of Brucella abortus. This glycosyltransferase has been called BABLpcC by the inventors. In particular, the inventors have shown that, contrary to all mutants of the LPS core described to date which induce the deletion of the core and of the O-chain of the LPS (Gonzales et al.; PLOS one, July 2008, vol. 3, issue 7, e2760), the mutant Gram-negative bacteria according to the invention present a LPS which lacks part of the core but keeps an intact O-chain. These results evidence that Brucella abortus possesses a branched LPS core, which was unknown to date (sec FIG. 10, which gives a proposed structure of the core of the LPS of Brucella abortus). Without wanting to be bound by a theory, it is believed that this branched structure of core of the LPS in the wild type bacteria is important in avoiding recognition by innate immunity. Consequently, the Gram negative bacteria mutants according to the invention trigger a more intense and protective immune response, and thus constitute very promising vaccines.

In addition to the BABLpcC of Brucella abortus, the inventors have also shown that homologous glycosyltransferases exist in other organisms. As a result, it is highly credible that the particular structure of the core of the LPS of Brucella abortus exists in other organism. The inventors have further shown that these homologous proteins have an amino acid sequence presenting a high percentage of identity with SEQ ID NO:1, of at least 60%, particularly of at least 70%, more particularly of at least 80%.

Examples of glycosyltransferases involved in the synthesis of the core of the LPS and having a high percentage of identity with BABLpcC are presented in the table hereinafter:

Organism SEQ ID NO: % identity with SEQ ID NO: 1 Bartonella quintana 2 65 Bartonella tribocorum 3 64 Bartonella bacilliformis 4 61 Ochrobactrum anthropi 5 85 Ochrobactrum intermedium 6 85 Agrobacterium tumefaciens 7 63 Bartonella henselae 22 69

Hence, in a particular embodiment, the invention also concerns the gram-negative bacterium according to the invention wherein said amino acid sequence having at least 60%, particularly at least 70%, more particularly at least 80% of identity with SEQ ID NO: 1 is selected from the group comprising SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7 and SEQ ID NO:22.

In addition to the glycosyltransferase of SEQ ID NO:1, the inventors have shown that another glycosyltransferase, having the sequence of SEQ ID NO:21, is also involved in the synthesis of the branched structure of the core of the LPS of a Gram-negative bacterium, Brucella abortus. The inventors have also shown that homologous glycosyltransferases exist in other organisms, as previously described for BABLpcC. The inventors have further shown that these homologous proteins have an amino acid sequence presenting a percentage of identity with SEQ ID NO:21 of at least 50%, particularly of at least 60%, more particularly of at least 62%.

Examples of glycosyltransferases involved in the synthesis of the core of the LPS and having a percentage of identity with SEQ ID NO:21 of at least 50%, particularly of at least 60%, more particularly of at least 62% are presented in the table hereinafter:

Organism SEQ ID NO: % identity with SEQ ID NO: 21 Ochrobactrum anthropi 23 62 Ochrobactrum intermedium 24 62 Agrobacterium radiobacter 25 57

In another particular embodiment, the invention also concerns the Gram-negative bacteria according to the invention wherein a gene encoding a protein involved in the synthesis of the O-polysaccharide of the LPS is inactivated. Indeed, in addition to the inactivation of genes encoding glycosyltransferases involved in the synthesis of the branched structure of the core of the LPS, it is of interest to inactivate genes involved in the synthesis of the O-polysaccharide of the LPS. Such a “double mutant”, lacking the branched structure of the core and partially or totally lacking the O-chain, is useful for distinguishing animals that are vaccinated with it and animals that are infected with the naturally occurring Gram-negative bacterium (wild type), as explained hereafter in the description.

Examples of genes encoding a protein involved in the synthesis of the O-polysaccharide of the LPS are wboB, wboA, wbkE, wbkA, gmd, per, wzm, wzt, wbkB, wbkC, wbkF and wbkD (Gonzales et al.; PLOS one, July 2008, vol. 3, issue 7, e2760). Their SEQ IDs are given in the table hereinafter:

Gene name Predicted protein function Amino acid SEQ ID wboB Mannosyl (perosaminyl) 8 transferase wboA Mannosyl (perosaminyl) 9 transferase wbkE Mannosyl (perosaminyl) 10 transferase wbkA Mannosyl (perosaminyl) 11 transferase gmd GDP-mannose dehydratase 12 per Perosamine synthetase 13 wzm ABC transporter 14 wbkF Undecaprenyl-glycosyltransferase 15 wbkD Epimerase/dehydratase 16 wzt ABC transporter 26 wbkB Synthetase 27 wbkC Formyltransferase 28

Accordingly, in an embodiment of the invention, said protein involved in the synthesis of the O-polysaccharide of the LPS is thus selected from the group comprising the proteins having the amino acid sequence of SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:26, SEQ ID NO:27 and SEQ ID NO:28 or homologues thereof having an amino acid sequence having at least 50%, particularly at least 60%, more particularly at least 70%, still particularly at least 80% and most particularly at least 90% of identity with an amino acid sequence selected from the group comprising SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:26, SEQ ID NO:27 and SEQ ID NO:28. The choice of a percentage of identity of at least 50% is not arbitrary: this percentage of identity has been found by the inventors for the homologous sequences of SEQ ID NO:8-16, 26-28 in the particular strain Yersinia enterocitica O:9.

In a particular embodiment of the invention, said protein involved in the synthesis of the O-polysaccharide of the LPS is a perosamine synthetase having the amino acid sequence of SEQ ID NO:13 or a homologue thereof having an amino acid sequence having at least 90% of identity with the amino acid sequence of SEQ ID NO:13. This high percentage of identity (of at least 90%) is typically found in the strains of the genus Brucella.

According to the invention, by “inactivated gene” it is meant a gene that encodes either a non-functional protein or no protein at all. According to the invention the inactivation of a gene can be carried out by the various methods known by the skilled person. Examples of methods for inactivating a gene are the knock out, and particularly the directed mutagenesis or the homologous recombination, as described in Conde-Alvarez R. et al., Cell Microbial 2006 August; 8(8):1322-35. A particular method for inactivating a gene according to the invention is described in the experimental section.

In another particular embodiment of the invention, the Gram-negative bacteria according to the invention are selected from the group comprising the bacteria of the genus Brucella, Bartonella, Ochrobactrum and Agrobacterium.

In a particular embodiment, the invention is directed to a bacterium of the genus Brucella, wherein said glycosyltransferase is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO: 1 or SEQ ID NO:21, or homologues thereof having an amino acid sequence having at least 60%, particularly at least 70%, more particularly at least 80% of identity with SEQ ID NO:1 or SEQ ID NO:21.

Particular species of the genus Brucella according to the invention are Brucella melitensis, Brucella abortus, Brucella suis, Brucella ovis, Brucella pinnipedialis, Brucella ceti, Brucella microti, and Brucella canis.

Particular species of the genus Ochrobactrum according to the invention are Ochrobactrum anthropi and Ochrobactrum intermedium.

The invention further concerns in particular a Ochrobactrum anthropi bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:5 or an amino acid sequence having at least 85% of identity with SEQ ID NO:1, or having the amino acid sequence of SEQ ID NO:23 or an amino acid sequence having at least 62% of identity with SEQ ID NO:21.

The invention further concerns in particular a Ochrobactrum intermedium bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:6 or an amino acid sequence having at least 85% of identity with SEQ ID NO:1 or having the amino acid sequence of SEQ ID NO:24 or an amino acid sequence having at least 62% of identity with SEQ ID NO:21.

Particular species of the genus Bartonella according to the invention are Bartonella henselae, Bartonella quintana, Bartonella tribocorum, Bartonella bacilliformis.

The invention also concerns in particular a Bartonella henselae bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:22, or an amino acid sequence having at least 69% of identity with SEQ ID NO:1.

The invention also concerns in particular a Bartonella quintana bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:2 or an amino acid sequence having at least 65% of identity with SEQ ID NO:1.

The invention still concerns in particular a Bartonella tribocorum bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:3, or an amino acid sequence having at least 64% of identity with SEQ ID NO:1.

The invention also concerns in particular a Bartonella bacilliformis bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:4, or an amino acid sequence having at least 61% of identity with SEQ ID NO:1.

Particular species of the genus Agrobacterium according to the invention are Agrobacterium tumefaciens and Agrobacterium radiobacter.

The invention thus concerns in particular an Agrobacterium tumefaciens bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:7 or an amino acid sequence having at least 63% of identity with SEQ ID NO:1.

The invention further concerns in particular an Agrobacterium radiobacter bacterium, wherein said glycosyltransferase according to the invention is selected from the group comprising the glycosyltransferases having the amino acid sequence of SEQ ID NO:25 or an amino acid sequence having at least 57% of identity with SEQ ID NO:21.

As used herein, the percentage of sequence identity refers to comparisons among amino acid sequences, and is determined by comparing two optimally aligned sequences over a comparison window, wherein the portion of the amino acid sequence in the comparison window may comprise additions or deletions (i.e., gaps) as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage may be calculated by determining the number of positions at which the identical amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity. Alternatively, the percentage may be calculated by determining the number of positions at which either the identical amino acid residue occurs in both sequences or an amino acid residue is aligned with a gap to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity. Those of skill in the art appreciate that there are many established algorithms available to align two sequences. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith and Waterman, 1981, Adv. Appl. Math. 2:482, by the homology alignment algorithm of Needleman and Wunsch, 1970, J. Mol. Biol. 48:443, by the search for similarity method of Pearson and Lipman, 1988, Proc. Natl. Acad. ScL USA 85:2444, by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the GCG Wisconsin Software Package), or by visual inspection (see generally, Current Protocols in Molecular Biology, F. M. Ausubel et al., eds., Current Protocols, a joint venture between Greene Publishing Associates, Inc. and John Wiley & Sons, Inc., (1995 Supplement) (Ausubel)). Examples of algorithms that are suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al., 1990, J. Mol. Biol. 215: 403-410 and Altschul et al., 1977, Nucleic Acids Res. 3389-3402, respectively. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information website. This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as, the neighborhood word score threshold (Altschul et al, supra). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are then extended in both directions along each sequence for as far as the cumulative alignment score can be increased. For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment. The BLASTP program (for amino acid sequences) uses as defaults a wordlength (W) of 3, an expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff and Henikoff, 1989, Proc Natl Acad Sci USA 89: 10915). Exemplary determination of sequence alignment and % sequence identity can employ the BESTFIT or GAP programs in the GCG Wisconsin Software package (Accelrys, Madison Wis.), using default parameters provided.

The invention also concerns the therapeutic applications of the Gram-negative mutants according to the invention. In particular, the invention related to the gram-negative bacterium according to the invention for use in a method for treatment of the human or animal body.

In another aspect, the invention relates to vaccines comprising a gram-negative bacterium according to the invention.

Indeed, the inventors have shown that the bacteria according to the invention can be used as live vaccines.

The invention thus relates to the gram-negative bacterium according to the invention, for use in a method for vaccinating the human or animal body against a disease caused by the wild type of said gram-negative bacterium.

The invention also relates to a method for treating, in particular vaccinating, a subject against a disease caused by a gram-negative bacterium, said method comprising the step of administering an therapeutically effective amount of said gram-negative bacterium modified according to the invention.

In the context of the invention, the term “treating” or “treatment”, as used herein, means reversing, alleviating, inhibiting the progress of, or preventing the disorder or condition to which such term applies.

As used herein, “subject” refers to a human or animal that may benefit from the administration of a Gram-negative bacterium as recited herein.

By a “therapeutically effective amount” of a Gram-negative bacterium as described previously, is meant a sufficient amount to treat the disease, at a reasonable benefit/risk ratio applicable to any medical treatment.

A vaccine is defined herein as a biological agent which is capable of providing a protective response in an animal to which the vaccine has been delivered and is incapable of causing severe disease. The vaccine stimulates antibody production or cellular immunity against the pathogen causing the disease; administration of the vaccine thus results in immunity from the disease.

According to the invention, by a “wild type” it is meant a gram-negative bacterium wherein the previously described genes are active.

If desired, the live vaccines according to the invention may contain an adjuvant. Examples of suitable compounds and compositions with adjuvant activity are well known in the art. Furthermore, nucleic acid sequences encoding polypeptides for pharmaceutical or diagnostic applications, in particular immunomodulators such as lymphokines, interferons or cytokines, may be incorporated into the vaccine.

A vaccine according to the invention can be prepared by conventional methods such as those commonly used for the commercially available live attenuated vaccines. The vaccine may be administered by intramuscular, intradermal, subcutaneous or intranasal inoculation or injection in an amount which is effective to protect the animal against challenge by a virulent strain of Gram-negative bacterium. This amount may vary according to the animal being inoculated, taking into consideration the size and weight of the animal. The vaccine according to the invention comprises an effective dosage of the Gram-negative bacterium mutant as the active component, i.e. a sufficient amount of Gram-negative bacterium mutant that will induce immunity in the vaccinated animals, against challenge by the virulent Gram-negative bacterium. Immunity is defined herein as the induction of a significant higher level of protection in a population of animals against mortality and clinical symptoms after vaccination compared to an unvaccinated group. In particular, the vaccine according to the invention prevents a large proportion of vaccinated animals against the occurrence of clinical symptoms of the disease and mortality.

When providing a patient (human or animal) with live bacteria vaccines, the dosage of administered bacteria will vary depending upon such factors as the route of administration, patient's species, age, weight, height, sex, general medical condition, previous medical history, etc. In general, it is desirable to provide the recipient with a dosage of the above bacteria which is in the range of from about 10⁵ cfu/kg to 10⁸ cfu/kg (body weight of patient), although a lower or higher dosage may be administered.

In addition to the Gram-negative bacterium mutant, the invention can also include combination vaccines comprising a vaccine strain capable of inducing protection against another pathogen.

In a particular embodiment of the invention, the Gram-negative bacteria of the invention belong to the Brucella genus. In this embodiment, the invention relates to these Gram-negative bacteria for use in a method for treatment of brucellosis in the human or animal body. Indeed, the brucellae are facultative intracellular parasites that infect a variety of mammals and have a great impact in animal and human health worldwide. These gram-negative bacteria lack typical virulence factors and behave as stealthy parasites that avoid detection by innate immunity at the onset of infection, thus retarding an adaptive cellular response and making possible for this pathogen to reach sheltered intracellular niches. This ability is not related to an induction of regulatory cytokines such as IL-10 but rather to the failure of innate immunity pathogen-recognition receptors (PRRs) to identify the Brucella surface molecules that normally bear the cognate pathogen-associated molecular patterns (PAMP) (Barquero-Calvo E et al. (2007) PLoS ONE 2: e631), and in particular the LPS of these strains. The strains of the invention, which lack a particular portion of the core of the LPS, have been shown by the inventors to induce a strong immune response and are thus suitable for use as vaccine against brucellosis.

As described previously, in a particular embodiment, the invention also concerns Gram-negative bacteria lacking the branched structure of the core and partially or totally lacking the O-chain. These double mutant bacteria are useful for distinguishing animals that are vaccinated with said double mutant bacteria and animals that are infected with the wild type Gram-negative bacteria.

The invention thus concerns a method for determining Gram-negative bacteria infection in an animal comprising the step of examining a sample obtained from said animal for the presence or absence of antibodies reactive with the immunodominant epitopes (C, C/Y, A and M or combinations thereof) of the O-chain (Alton, G. G. et al. 1988, Techniques for the brucellosis laboratory—INRA, Paris, France; Gall, D. et al. 2004, Rev. Sci. Tech. 23:989-1002). The sample of the animal used in this method may be any sample in which said antibodies can be detected, e.g. a blood, serum or tissue sample.

The presence or the absence of antibodies can be detected by any immunoassay known by the person skilled in the art. The design of this immunoassay may vary. For example, the immunoassay may be based upon competition or direct reaction. Furthermore, protocols may use solid supports or may use cellular material. The detection of the antibody-antigen complex may involve the use of labeled antibodies; the labels may be, for example, enzymes, fluorescent, chemiluminescent, radioactive or dye molecules. Suitable methods for the detection of the above mentioned epitopes in the sample include, for example, the enzyme-linked immunosorbent assay (ELISA), immunofluorescent tests and Western blot analysis.

In another aspect, the invention concerns an isolated lipopolysaccharide obtainable from a gram-negative bacterium according to the invention. Indeed, the inventors have found that the modified LPS produced by the Gram-negative bacteria according to the invention stimulate an unspecific production of cytokines, in particular of IL 12 and TNFα, by dentritic cells (FIG. 6B) in the mouse.

The LPS can be extracted from the Gram-negative bacteria according to the invention following any method known by the skilled person, as for instance the method described in Garin-Bastuji B et al. (1990) J Clin Microbiol 28: 2169-2174; Leong D et al. (1970) Infection and Immunity 1: 174-182; and Velasco, J., J. A. Bengocchea, K. Brandenburg, B. Lindner, U. Seydel, D. Gonzalez, U. Zähringer, E. Moreno, and I. Moriyón. 2000. Brucella abortus and its closest phylogenetic relative, Ochrobactrum spp., differ in outer membrane permeability and cationic peptide resistance. Infect. Immun. 68:3210-3218.

As a result, in one embodiment, the modified LPS according to the invention can be used in a method for stimulating the immune system of the human or animal body.

In another embodiment, the invention concerns an adjuvant comprising a lipopolysaccharide according to the invention.

In addition, the invention concerns a vaccine comprising an antigen and an adjuvant wherein said adjuvant comprises a lipopolysaccharide according to the invention. According to this embodiment, the LPS according to the invention enhances the immune response induced by the antigen comprised in the vaccine.

In another embodiment of the invention, the LPS according to the invention is conjugated with a carrier molecule, in order to enhance its immunogenicity. The invention thus concerns a conjugate comprising a lipopolysaccharide obtainable from a gram-negative bacterium according to the invention linked to a carrier molecule. According to this embodiment, the LPS/carrier conjugate induces a specific immune response against the LPS and can thus be used as a vaccine. Non limitative examples of carrier molecules are carrier proteins, such as the tetanus toxoid or the diphtheria toxoid.

Further aspects and advantages of this invention will be disclosed in the following figures and examples, which should be regarded as illustrative and not limiting the scope of this application.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1: The BABΔlpcC has a defect in the LPS core. SDS-PAGE of phenol-water extracts and Western blot analysis of LPS SDS-proteinase K extracts from BAB-parental (Ba wt-LPS), BABΔlpcC (Ba LpcC-LPS), and BABΔlpcCplpcC (Ba LpcC-compl-LPS) strains. The Moabs used were Cby-33H8 (to C/Y epitope of the O-chain) and A68/24D08/G09.

FIG. 2: Aggregate state of Ba wt-LPS and Ba LpcC-LPS. (A), aggregate size of the major and minor LPS fractions on dependence of concentration measured by light scattering. (B), determination of the critical aggregate concentration by fluorescence emission of NPN (the increase in fluorescence caused by the partition of NPN into the aggregates starts at 10 μg/mL for both Ba wt-LPS and Ba LpcC-LPS). Same values were obtained for minor fractions.

FIG. 3: BABΔlpcC shows increased sensitivity to the killing action of normal serum that relates to the LPS defect. (A), survival of BAB-parented, BABΔlpcC, BABTn5::per and BABTn5::bvrR after incubation in non-immune serum for 90 min. Data are the media±standard error of three simultaneous measurements (the results shown are representative of three independent experiments); (B), gel to liquid crystalline (β⇄α) phase transition of the hydrocarbon chains of Ba wt-LPS and Ba LpcC-LPS in presence or absence of normal human serum. The position of the peak of the symmetric stretching vibration of the methylene groups vs(CH2) versus temperature is plotted.

FIG. 4: BABΔlpcC shows increased sensitivity to polycationic bactericidal peptides that relates to the LPS defect. (A), MICs determined by the E-test (colistin) or serial dilution method (polymyxin B, poly-L-ornithine, poly-L-lysine). The results shown are representative of three experiments in which of BAB-parental, BABΔlpcC where assayed simultaneously; (B), gel to liquid crystalline (β⇄α) phase transition of the hydrocarbon chains of Ba wt-LPS and Ba LpcC-LPS in presence or absence of polymyxin B at a LPS:PMB 1:0.1 molar ratio. The position of the peak of the symmetric stretching vibration of the methylene groups vs(CH2) versus temperature is plotted.

FIG. 5: BABΔlpcC is attenuated in dendritic cells but not in macrophages. (A), Kinetics of intracellular survival and replication of BAB parental, BABΔlpcC and BABΔlpcC-plpcC in BMDM (left panel) or BMDC (right panel) (a virB10::Gm mutant attenuated in both types of cells is included as a reference; each point represents the mean±standard error of triplicate wells of one representative experiment [three independent experiments were performed]); (B), confocal images of BMDCs infected with BAB parental GFP or BABΔlpcC GFP (clear grey) labeled with Moabs to either calnexin, or LAMP 1 (both in dark grey) 24 hours after infection.

FIG. 6: BABΔlpcC stimulates a comparatively increased cytokine release in infected BMDC that is paralleled by the TLR4-dependent activity of the Ba LpcC-LPS. (A), cytokine levels in the supernatants (24 h incubation) of infected (left panel) of LPS stimulated (right panel) BMDC obtained from TLR wild type mice; (B), cytokine levels in the supernatants (24 h incubation) of LPS stimulated BMDC obtained from TLR ko mice. Codes for the bacteria and LPSs are those used in the text. Values correspond to mean±standard error of at least three independent experiments.

FIG. 7: Ba LpcC-LPS shows a comparatively increased binding to h-MD2.

FIG. 8: BABΔlpcC stimulates a dendritic cell maturation. The figure shows the percentages of BMDCS infected with either BAB-parental, BABΔlpcC or S. typhimurium that contain DALIS.

FIG. 9: BABΔlpcC attenuated in mice. The plots show the infection kinetics in the spleens (left panel) and the spleen weights (right panel) of mice inoculated with BAB-parental or BABΔlpcC (each point is the mean±standard error [n=5] of the logarithm of CFU). The plots of the B. abortus S19 reference vaccine and of the O-chain deficient BABTn5::per obtained in an independent experiment are added as a reference.

FIG. 10: Proposed representation of the core of Brucella LPS. In this representation, the branched structure of the core is represented with two sugar units (alpha-D-Manp and beta-D-GlcpN). The core is linked to lipid A through a Kdo I sugar unit, whereas it is linked to the O-chain through an alpha-D-Glcp. This representation is given with a comprehension purpose only and does not bind the inventors with any theory since the exact structure of the core is still unknown to date.

FIG. 11. Regression analysis of the kinetics of spleen clearance of BABΔlpcC and of its parental strain. The corresponding regression equations (y=−0.27x+6.81 [R=0.77] and y 0−0.07x+6.85 [0.95]) predict a clearance time of 25.2 and 93.8 weeks for BABΔlpcC and BAB-parental, respectively. Each point represents the mean±standard error of the logarithm of CFU in the spleens of five animals.

EXAMPLES

In the following description, all molecular biology experiments for which no detailed protocol is given are performed according to standard protocols.

Material and Methods Bacterial Strains and Growth Conditions.

The bacterial strains and plasmids used are listed in Table 1:

TABLE 1 Bacterial strains and plasmids Strain/plasmids Relevant characteristics Reference/Source Brucella abortus B. abortus 2308 Wild type, virulent, biotype 1, S-LPS. BAB-parental Nal^(R) spontaneous mutant of strain B. abortus 2308 (Sangari and Agüero 1991) BABΔlpcC BAB-parental.lpcC_(Δ16-308) This work BABΔlpcC-plpcC BABΔlpcC harboring plasmid plpcC This work BABTn5::per 2308 NalR per::Tn5; rough-LPS (Monreal et al. 2003) virB10::Gm 2308 NalR Gm^(R), nonpolar mutant of virB10 (Sieira et al. 2000) BAB-Tn5::bvrR BAB-parental bvrR::Tn5, S-LPS; fully attenuated; Mutant 65.21 in Sola- sensitive to normal serum Landa et al. 1998) BAB-parental GFP BAB-parental harboring pBBR1MCS-2 GFP Km^(R) This work BABΔlpcC GFP BABΔlpcC harboring pBBR1MCS-2 GFP Km^(R) This work B. abortus S19 Dr. J.M. Blasco, C.I.T.A. Gobierno Aragón. E. coli S17-1 Mating strain with plasmid RP4 inserted into the (Simon et al. 1983) chromosome Top10 F F-Iaclq Tn 10 (Teir) mcrA Δ(mrr-hsdRMS-mcrBC) Invitrogen 80lacZΔM15 ΔlacX74 recA1alaD139 Δ (ara-leu)7697 galU galK rpsL endA1 nupG Plasmids pCR2.1 Cloning vector Invitrogen pJQK Derivative of pJQ200KS +; Km^(R); Gm^(S) (Scupham and Triplett 1997) pRH001 Derivative of pMR10 Km^(R); Cm^(R) (Hallez et al. 2007) pRCI-23 1019-bp of BAB-parental chromosomal DNA This work containing the lpcC deletion allele, generated by PCR and cloned into pCR2.1 pRCI-26 BamHl-Xbal fragment from pRCLl-23 cloned into the This work corresponding sites of pJQK pDONR201 B. melitensis chromosomal DNA containing the (Dricot et al. 2004) BMEl0509 complete lpcC gene, generated by PCR and cloned into pDONR201 (Invitrogen) plpcC attL1-attL2 fragment of pDONR201-BMEl0509 This work cloned into the attR1-attR2 sites of pRH001 pBBR1MCS-2 GFP pBBR1MCS-2 derivative expressing the gfp-mut3 Dr. J.P, Garver, INSERM- gene under the control of the lack promoter CNRS, Marseille, France.

Bacteria were routinely grown in standard tryptic soy broth or agar either plain or supplemented with kanamycin at 50 μg/ml, or/and nalidixic at 25 μg/ml, or/and 5% sucrose. All strains were stored in skim milk at −80° C.

LPS Extraction and Characterization.

Extraction of whole-cell LPS by SDS-proteinase K protocol was performed as described previously (Garin-Bastuji B et al., (1990) J Clin Microbial 28: 2169-2174). In addition, LPS was obtained by methanol precipitation of the phenol phase of a phenol-water extract (Leong D et al. (1970) Infection and Immunity 1: 174-182). This fraction (10 mg/mL in 175 mM NaCl, 0.05% NaN3, 0.1 M Tris-HCA [pH 7.0]) was then purified by digestion with nucleases (50 μg/ml each of DNase-II type V, and RNase-A [Sigma], 30 min at 37° C.) and three times with proteinase K (50 μg/ml, 3 hours at 55° C.), and ultracentrifuged (6 h, 100,000×g) (Aragon V et al. (1996) J Bacterial 178: 1070-1079). Free lipids (ornithine lipids and phospholipids) were then removed by a fourfold extraction with chloroform-methanol. (2:1 [vol/vol]) (Velasco 1 et al. (2000) Infect Immun 68: 3210-3218).

LPSs were analyzed in 15 or 18% polyacrylamide gels (37.5:1 acrylamide/methylene-bisacrylamide ratio) in Tris-HCl-glycine and stained by the periodate-alkaline silver method (Tsai C M et al. (1982) Anal Biochem 119: 115-119). For Western blots, gels were electrotransferred onto nitrocellulose sheets (Schleicher & Schuell GmbH, Dassel, Germany), blocked with 3% skim milk in 10 mM phosphate-buffered saline (PBS) with 0.05% Tween 20 overnight, and washed with PBS-0.05% Tween 20. Immune sera were diluted in this same buffer and, after incubation overnight at room temperature, the membranes were washed again. Bound immunoglobulins were detected with peroxidase-conjugated goat anti-mouse immunoglobulin (Nordic) and 4-chloro-1-naphthol-H₂O₂. Monoclonal antibodies (Moabs) used in this study were Cby-33H8 (Ingenasa, Madrid, Spain), which recognizes the C/Y O-chain epitope, and A68/24D08/G09, A68/24G12/A08, and A68/3F03/D5 which recognize core epitopes (Bowden R A et al. (1995) Infection and Immunity 63: 3945-3952). The inner core LPS marker 3-Deoxy-D-manno-2-octulosonic acid (Kdo) was determined calorimetrically by the thiobarbituric acid method using pure Kdo and deoxyribose as the standards, with the modifications described previously (Díaz-Aparicio E et al. (1993) J Clin Microbiol 31: 3136-3141; Díaz-Aparicio E et al. (1993) J Clin Microbiol 31: 3136-3141).

Determination of the Aggregate Size and Critical Aggregation Concentration of LPS.

The aggregate size of LPSs was determined by dynamic light scattering. Stock LPS suspensions were prepared at 1 mg/mL in deionized, reverse osmosis purified water and subjected to three cycles of heating to 56° C. and cooling to 4° C. to homogenize them. On the day of use, serial dilutions in the range 1 to 500 μg/mL were prepared and filtered through 0.45 μm, low protein binding Durapore® (PVDF) membranes immediately before measuring. Light scattering measurements were carried out in a DynaPro apparatus at 37° C. using a laser of 825 nm and 90° scattering angle. The data were analyzed by the regularization method in the Dynamics V6 software.

The critical aggregation concentration of LPS was determined by steady-state fluorescence using N-phenyl-1-naphthylamine (NPN), a hydrophopic fluorescent probe, whose quantum yield increases in hydrophobic environments. NPN (500 μM in acetone) was added into 1 mL of water to reach NPN at 15 μM final concentration in a quartz cuvette 1 cm optical. Then different volumes from a stock of LPS were added (from 1 μg/mL to 100 μg/mL, final concentration). Fluorescence was measured (excitation, 350 nm; emission scan, 380 nm-600 nm) in Edinbugrh FLS920 apparatus at 37° C.

Determination of the Acyl-Chain Fluidity of LPS.

The transition of the acyl chains of LPS from a well-ordered state (gel phase) to a fluid state (liquid crystalline phase) at a lipid-specific temperature (Tc) was determined by Fourier transform infrared spectroscopy. A specific vibrational band, the symmetric stretching vibration of the methylene groups vs(CH2) around 2,850 cm⁻¹, was analyzed since its peak position is a measure of the state of order (fluidity) of the acyl chains (Brandenburg K et al. (1997) Biochim Biophys Acta 1329: 183-201). Measurements were performed in a Bruker IFS 55 apparatus (Bruker, Karlsruhe, Germany) as described previously (Brandenburg K et al. (1997) Biochim Biophys Acta 1329: 183-201). To ensure homogeneity, LPS suspensions were prepared in 2.5 mM HEPES (pH 7.2) at room temperature, incubated at 56° C. for 15 min, stirred, and cooled to 4° C. This heating cooling step was repeated three times, and the suspensions were stored at 4° C. for several hours before analysis. LPS suspensions (water content, 90%) were analyzed in CaF₂ cuvettes with 12.5-μm Teflon spacers, and for each measurement, 50 interferograms were accumulated, Fourier transformed, and converted to absorbance spectra. The measurements were obtained in continuous heating scans (2° C./min) between 10° C. and 60° C. To test the effect of complement, the experiments were performed in the presence of normal human serum. The effect of polymyxin B was assessed similarly at different LPS:polymyxin B molar ratios (see Results), and using an average MW of 11800 for B. abortus LPS (determined by SDS-PAGE with Yersinia enterocolitica O:8 LPS as a standard).

DNA Manipulations.

Plasmid and chromosomal DNA were extracted with Qiaprep spin Miniprep (Qiagen GmbH, Hilden, Germany), and Ultraclean Microbial DNA Isolation kit (Mo Bio Laboratories) respectively. When needed, DNA was purified from agarose gels using Qiack Gel extraction kit (Qiagen). DNA sequencing was performed by the Servicio de SecuenciaciOn de CIMA (Centro de Investigación Médica Aplicada, Pamplona, Spain). Primers were synthesized by Sigma-Genosys Ltd. (Haverhill, United Kingdom). Searches for DNA and protein homologies were carried out using the NCBI (http://www.ncbi.nlm.nih.gov) and the EMBL-European Bioinformatics Institute server (http://www.ebi.ac.UK/ebi_home.html). In addition, sequence data were obtained from The Institute for Genomic Research website at http://www.tigr.org. Genomic sequences of B. melitensis 16M, B. abortus and B. suis were analyzed using the database of the URBM bioinformatic group (http://www.serine.urbm.fundp.ac.be/˜seqbruce/GENOMES/Brucella_melitensis).

Construction of the B. abortus lpcC Non Polar Mutant (BABΔlpcC).

In-frame deletion mutant BABΔlpcC was constructed by PCR overlap using genomic DNA of B. abortus 2308 as DNA template. Primers were designed based on the available sequence of the corresponding genes in B. abortus 2308. For the construction of the lpcC mutant, we first generated two PCR fragments: oligonucleotides lpcC-F1 (5′-CTGGCGTCAGCAATCAGAG-3′; SEQ ID NO:17) and lpcC-R2 (5′-GTGCAACGACCTCAACTTCC-3′; SEQ ID NO:18) were used to amplified a 476-bp fragment including codons 1 to 16 of the lpcC ORF, as well as 424 bp upstream of the lpcC start codon, and oligonucleotides lpcC-F3 (5′-GGAAGTTGAGGTCGTTGCACACGCCATCGAACCTTATCTG-3′; SEQ ID NO:19) and lpcC-R4 (5′-CGGCTATCGTGCGATTCT-3′; SEQ ID NO:20) were used to amplify a 453-bp fragment including codons 308 to 354 of the lpcC ORF and 320-bp downstream of the lpcC stop codon. Both fragments were ligated by overlapping PCR using oligonucleotides lpcC-F1 and lpcC-R4 for amplification, and the complementary regions between lpcC-R2 and lpcC-F3 for overlapping. The resulting fragment, containing the lpcC deletion allele, was cloned into pCR2.1 (Invitrogen), to generate plasmid pRC1-23, sequenced to ensure the maintenance of the reading frame, and subsequently subcloned into the BamHI and the XbaI sites of the suicide plasmid pJQK (Scupham A J et al. (1997) Gene 202: 53-59). The resulting mutator plasmid (pRCI-26) was introduced in B. abortus 2308 bp conjugation. The first recombination (integration of the suicide vector in the chromosome) was selected by Nal and Kan resistance, and the second recombination (excision of the mutator plasmid leading to construction of the mutant by allelic exchange), was selected by Nal and sucrose resistance and Kan sensitivity. The resulting colonies were screened by PCR with primers lpcC-F1 and lpcC-R4 which amplify a fragment of 929 bp in the mutant and a fragment of 1805 bp in the parental strain. The mutation generated results in the loss of the 82% of the lpcC ORF, and the mutant strain was called BABΔlpcC.

Complementation of BABΔlpcC.

Taking into account that the LpcC sequences of B. melitensis and B. abortus are identical, we used the B. melitensis ORFeome constructed with the Gateway cloning Technology (Invitrogen) for complementation (Dricot A et al. (2004) Genome Res 14: 2201-2206). The clone carrying B. melitensis lpcC was extracted, and the DNA containing the corresponding ORF was subcloned in pRH001 (Hailez R et al. (2007) Appl Environ Microbiol 73: 1375-1379) to produce plasmid plpcC. To complement the lpcC mutation, plasmid plpcC was introduced into the BABΔlpcC mutant by mating with E. coli S17-1 and the conjugants harbouring piper (designated as BABΔlpcCplpcC) were selected by plating the mating mixture onto TSA-Nal-Kan plates which were incubated at 37° C. for 3 days.

Sensitivity to Brucellaphages, Dyes, Antibiotics and Polycationic Bactericidal Peptides

The minimal inhibitory concentrations (MICs) of polymyxin B, poly-L-ornithine, poly-L-lysine, colistin, penicillin, doxycycline, clarithromycin, erythromycin, rifampicin, basic fuchsin, safranin and thionine was determined in Müller-Hinton medium by standard procedures. Sensitivity to the S (Wb, Iz) and rough (R/C)-specific brucellaphages was measured by testing the lysis of bacteria exposed to serial 10-fold dilutions made from a routine test dilution phage stock (Alton G G et al. (1988) Techniques for the brucellosis laboratory. Paris, France: INRA).

Sensitivity to the Bactericidal Action of Nonimmune Serum.

Exponentially growing bacteria were adjusted to 10⁴ CFU/ml in saline and dispensed in triplicate in microtiter plates (45 μl per well) containing fresh normal bovine serum (90 μl/well). After 90 min of incubation at 37° C., brain heart infusion broth was dispensed (200 μl/well), mixed with the bacterial suspension and 100 μl was plated on tryptic soy agar. Results were expressed as the percentage of the average CFU with respect to the inoculum.

Intracellular Multiplication.

Bone marrow cells were isolated from femurs of 7-8-week-old C57Bl/6 female, TLR4^(/) (Hoshino K et al. (1999) J Immunol 162: 3749-3752) or TLR9−/− (Hemmi H et al. (2000) Nature 408: 740-745) mice and differentiated into either dendritic cells (BMDCs) or macrophages (BMDM) as described by Inaba et al. or De Chastellier et at (Inaba K et al. (1992) J Exp Med 176: 1693-1702; Inaba K et al. (1992) J Exp Med 176: 1693-1702; De Chastellier C et al. (1993) Infect Immun 61: 3775-3784), respectively. Infections were performed by centrifuging the bacteria onto the differentiated cells (400×g for 10 min at 4°; bacteria: cells ratio of 20:1 for BMDCs or 50:1 for BMDM) followed by incubation at 37° C. for either 15 min (BMDM) or 30 min (BMDCs) under a 5% CO₂ atmosphere. Cells were either extensively washed (BMDM) or gently washed (BMDCs) with medium to remove extracellular bacteria and incubated in medium supplemented with 100 μg/ml gentamycin for 1 h to kill extracellular bacteria. Thereafter, the antibiotic concentration was decreased to 20 μg/ml. To monitor Brucella intracellular survival, infected cells were lysed with 0.1% (vol/vol) Triton X-100 in H2O (BMDCs) or after PBS washing (BMDM) and serial dilutions of lysates were rapidly plated onto tryptic soy agar plates to enumerate CFUs.

Immunofluorescence Assays.

BMDCs were grown on glass coverslips and inoculated with bacteria as described above. At different times after inoculation (see Results), coverslips were fixed with 3% paraformaldehyde pH 7.4 at 37° C. for 15 min and washed three times with PBS. Coverslips were processed for immunofluorescence staining as previously described (Celli J et al. (2003) J Exp Med 198: 545-556). Briefly, cells were permeabilized with 0.1% saponin and incubated with primary antibodies. After several washes, the primary antibodies were revealed with the appropriate secondary antibodies. The primary antibodies used for immunofluorescence microscopy were: cow anti-B. abortus; rat anti-mouse LAMP 1 ID4B (Developmental Studies Hybridoma Bank, National Institute of Child Health and Human Development, University of Iowa); mouse anti FK2 (Biomol) and Moab anti-calnexin (kindly provided by Dr. D. Williams, University of Toronto). In all experiments, BMDCs were labeled using an antibody against a conserved cytoplasmic epitope found on MHC-II 1-A β subunits (Lelouard H et al. (2002) Nature 417: 177-182) which does not produce significant labeling with BMDM and were also labeled with an anti-CD11c antibody (Biolegend) confirming that they are DCs (Salcedo S P et al. (2008) PLoS Pathogens 4: e21). Samples were analyzed under a Leica DMRBE epifluorescence microscope for quantitative analysis, or a Zeiss LSM 510 laser scanning confocal microscope for image acquisition.

Cytokine Measurement.

Sandwich enzyme-linked immunosorbent assays (ELISA) (AbCys, Paris, France) were used to detect IL-12 (p40/p70) and TNFα in the supernatants of BMDCs 24 hours after infection (see above) or after stimulation with 10 μg/ml of the appropriate LPS from different Brucella strains or 100 ng/ml from E. coli ATCC 35218 obtained by the phenol-water procedure and purified further by the phenol-water-deoxycholate method. For the latter purpose, a stock of 1 mg/ml in pyrogen free sterile water was prepared, sonicated briefly and sterilized by autoclaving. Prior to use, the stock was heated at 56° C. for 15 min and then cooled to room temperature.

LPS Binding to hMD-2 by Competitive ELISA.

The ELISA for determination of LPS binding to hMD-2 was performed in 96-well plates (NUNC immunoplate F96 cert. Maxi-sorp). Chicken anti-hMD2 (GenTel) (5 μg/mL) in 50 mM Na₂CO₃ (pH 9.6) was used to coat the microtiter plate at 4° C. overnight. Excess binding sites were blocked with 1% BSA in 10 mM PBS buffer (pH 7.2) for 1 h at room temperature, and rinsed three times with the same buffer. During the blocking step, hMD-2 (0.75 μM) was preincubated with 0 μM to 8 μM LPS at 37° C. and, as a negative control, LPS was also preincubated in absence of hMD2. This preincubated solutions were added to the plate, which was then incubated for 1 h at 37° C. After rinsing, hMD-2 not bound to LPS was detected by incubation with 0.1 μg/ml of mouse anti h-MD2 (clone 9B4 e-Bioscience) in 10 mM PBS buffer at 37° C. for 1 h, followed by incubation with 0.1 μg/ml peroxidase-conjugated goat anti-mouse IgG (Santa Cruz), also in PBS buffer at 37° C. for 1 h. After plate washing, ABTS (Sigma) was added, the reaction was stopped with 1% SDS after 15 min, and the absorbance at 420 nm measured using a Mithras LB940 apparatus. (Berthold Technologies).

Virulence Assay in Mice.

Infection experiments were performed as described in Conde-Alvarez, R. et al., 2006, Cell. Microbiol. 8:1322-1335. For each strain, 30 mice were inoculated intraperitoneally with 0.1 mL of inoculum containing 5.8×10⁴ (parental control) and 4.9×10⁴ (BABΔlpcC) CFU/mouse and the number of CFU in spleens (n=5) was determined at 1, 2, 4, 6, 8, and 12 weeks after inoculation. The identity of the spleen isolates was confirmed by PCR at several points during the infection process. The individual data were normalized by logarithmic transformation, and the mean and standard deviation of log CFU/spleen were calculated. Statistical comparisons were performed by the Fisher's Protected Least Significant Differences test. An additional infection was performed under the same conditions but including BABΔlpcC harboring plpcC. The number of CFU in spleens was determined 8 weeks after inoculation.

Protection Studies in Mice.

Three groups of 10 mice each were inoculated subcutaneously with 3.9×10⁴ CFU of BABΔlpcC, 1.3×10⁵ of B. abortus S19 per mouse, or sterile saline as a control. Four weeks after vaccination, each group was challenged by intraperitoneal injection of 3.6×10⁴ CFU of virulent B. abortus per mouse. To differentiate the challenge from the vaccine strain, BAB-parental GFP (Table 1) was used taking advantage of its kanamycin resistance (in preliminary experiments, the virulence of BAB-parental GFP was measured and found to be identical to that of BAB-parental). Two and six weeks later, mice were euthanized by cervical dislocation, and the CFU of the challenge strain in the spleens was determined on tryptic soy agar supplemented with kanamycin (see above). The mean±SD of the log CFU per spleen was calculated and statistical comparisons made as described above. The vaccine and challenge doses, routes, and challenge intervals were chosen on the basis of previous evidence (Grillo M J et al. (2000) Biologicals 28: 119-127; Stevens M G et al, (1995) Infection and Immunity 63: 264-270).

Results

Construction and Characteristics of a B. abortus lpcC Mutant. To analyze the role of ORF BAB1_(—)1522 in the synthesis of Brucella LPS, we constructed a non-polar mutant (BABΔlpcC) by making an in frame internal deletion of the region coding for amino acids 17 to 307. To test if the mutation induced cell envelope modifications or changes in the permeability pattern characteristic of Brucella (Martinez de Tejada G et al. (1993) J Bacteriol 175: 5273-5275), we compared the sensitivity of the BAB-parental strain and the BABΔlpcC mutant to S and R brucellaphages, dyes (fuchsin, thionine and safranine) and hydrophobic (erythromycin, rifampicine) and hydrophilic (penicillin, doxycycline, clarithromycin) antibiotics. Both strains behaved similarly in all tests performed and, moreover, showed similar growth rates (data not shown). the BABΔlpcC Mutant has a Defect in the LPS Core.

To analyze the effect of the lpcC mutation in the LPS structure, we extracted this molecule using the protocol developed for Brucella S-LPS (Leong D et al. (1970) Infection and Immunity 1: 174-182). This protocol includes a phenol-water partition followed by first digestion with nucleases and proteinase K and then ultracentrifugation, a step that allows the recovery of over 70% of the purified LPS in the sediment. Then, the LPS is freed from phospholipids and ornithine lipids by solvent extraction. However, when this method was applied to BABΔlpcC, the yield was only a 32% of that obtained with the parental strain, a result that could be due to either a diminished amount of LPS in BABΔlpcC, or to a failure of the standard protocol to yield the LPS quantitatively. The first possibility was ruled out by measuring the whole bacterial LPS content using the SDS-proteinase K extraction method followed by Western blot with anti-O-chain Moab Cby-33H8 (C/Y specificity) (FIG. 1). When we reexamined the classical protocol, we found that the supernatant of the ultracentrifugation contained an unexpected amount of a material. By SDS-PAGE and Kdo analysis this material was similar to the S-LPS obtained in smaller amounts in the sediment of the ultracentrifugation step (not shown). These results suggested a different aggregation state in the parental and the BABΔlpcC S-LPSs, a possibility tested by measuring the aggregate size by dynamic light scattering. Both for the parental and BABΔlpcC S-LPSs, the aggregates in the supernatant fractions had an average ratio of ca. 100 nm whereas those in the sediment were of ca. 150 nm at concentrations above 100 μg/mL (FIG. 2). This, however, did not relate to a difference in the critical aggregate concentration of these LPSs (10 μg/ml), as shown by fluorimetry (FIG. 2). These results showed that the major fractions of the LPS of BABΔlpcC and BAB-parental differed in aggregate size.

The SDS-PAGE and Western-blot analysis showed that, as expected, the parental strain contained a wild type LPS consisting of both S and R fractions (FIG. 1). However, although there was no change in the total S-LPS content, the BABΔlpcC LPS extracts had less amounts of R-LPS and with a different migration pattern from. This peculiarity, which was observed both in the supernatant (not shown) and the sediment fractions (FIG. 1), was corroborated by the lack of reactivity of the anti-core Moabs (FIG. 1) with LPS obtained from BABΔlpcC by the SDS-proteinase K procedure. Furthermore, when plasmid plpcC (encoding the lpcC gene) was introduced into BABΔlpcC the Moab reactivity was restored (FIG. 1). These results indicate that LpcC is required for the normal synthesis of the core LPS but not for the assembly and incorporation of the O-chain. Unless stated otherwise, the studies described below were performed with the major fractions of each bacteria (henceforth referred to as Ba wt-LPS and Ba LpcC-LPS).

An Intact LPS Core is Required for the Resistance of B. abortus to the Bactericidal Action of Polycationic Peptides and Normal Serum.

S. brucellae are resistant to the bactericidal action of normal serum, and this resistance has been attributed to the O-chain (Eisenschenk F C et al. (1999) Vet Microbiol 68: 235-244). However, some B. melitensis R mutants and B. ovis (a naturally R Brucella species) have been reported to be resistant to serum (David Gonzalez, Caro-Henandez, Fernandez-Prada), suggesting that the LPS core may also be important. To assess this possibility, BABΔlpcC, BABTn::5per, BABTn::5bvrR (Table 1) and BAB parental were incubated in normal serum for 90 minutes and tested for viability. As it can be seen in FIG. 3, BABΔlpcC was more sensitive than BAB-parental strain but not as much as bvrR mutant. Moreover, comparison with BABTn::5 per showed that the core was as important as the O-chain in this property.

The involvement of the defect in the Ba LpcC-LPS in the increased serum sensitivity of BABΔlpcC was tested. To this end, we examined the lipid A acyl chain fluidity of Ba wt-LPS and Ba LpcC-LPS in the presence of serum, since this parameter increases upon binding of molecules to the LPS aggregates (Brandenburg K et al. (2005) Biophys J 88: 1845-1858). As it is shown in FIG. 3, the β⇄α transition that marks the shift from the crystalline to the fluid phase took place in the 30 to 40° C. range for the Ba wt-LPS, with a Tc of 37° C. in the absence of serum. Surprisingly, the Ba LpcC-LPS showed a very different fluidity profile with a Tc between 45 and 55° C., and with a more restricted acyl chain fluidity below Tc than the Ba wt-LPS, showing that the aggregates were in the crystalline phase at physiological temperatures. Despite this greater rigidity, Ba LpcC-LPS aggregates were clearly affected by the presence of normal serum whereas those of Ba wt-LPS were not (FIG. 3). These results suggest that the lack of part of the core could be uncovering complement targets and are in agreement with the serum sensitivity of the bacteria.

Brucella is also resistant to bactericidal polycationic peptides (Martinez de Tejada G et al. (1995) Infect Immun 63: 3054-3061; Freer E et al. (1996) J Bacteriol 178: 5867-5876), a property linked mostly to the low negative charge in the core and lipid A LPS sections (Velasco J et al. (2000) Infect Immun 68: 3210-3218). To assess weather the core defect in BABΔlpcC affected this property, we examined the sensitivity to polymyxin B, colistin, poly-L-lysine, and poly-L-ornithine. The results demonstrated a greater sensitivity of BABΔlpcC to all these agents (FIG. 4). Like in the serum sensitivity experiments, the Ba LpcC-LPS was tested for polycation binding by measuring acyl chain fluidity. FIG. 4 shows that polymyxin B increased the fluidity of Ba LpcC-LPS.

An Intact LPS Core is Required for B. abortus to Evade Lysosome Fusion and to Multiply in Dendritic Cells.

BABΔlpcC was tested for their ability to multiply in bone marrow derived macrophages (BMDM) and dendritic cells (BMDCs) in comparison with BAB parental. The behavior in BMDM of both bacteria was similar thus showing no attenuation of the mutant in these cells (FIG. 5). In contrast, the attenuated virB mutant used as a control failed to multiply. In BMDCs, however, BABΔlpcC and BAB-parental showed a different behavior. Whereas BAB-parental was not destroyed and was able to multiply, BABΔlpcC decreased markedly either immediately after infection (FIG. 5A) or after 24 hours (not shown), depending upon the experiment, although not to the extent of the virB control. Complementation of BABΔlpcC with plasmid plpcC restored the ability to multiply in these cells. The intracellular location in BMDC was determined by confocal microscopy (FIG. 5B). Twenty-four hours after infection, BAB-parental was present in high number in BMDC whereas cells infected with BABΔlpcC were almost free of them. Moreover, the majority of BAB-parental bacteria colocalized with the endoplasmic reticulum marker calnexin, but not with the lysosomal marker LAMP-1. By contrast, the BABΔlpcC mutant was in LAMP1-positive vacuoles, apparently unable to establish an endoplasmic reticulum-derived compartment. Taken together, these results indicate that a higher proportion of mutant bacteria were degraded soon after uptake, showing that the LPS core has a role in the resistance of B. abortus to killing by dendritic cells.

The LPS Core Deficiency Increases TNFα and IL12 Secretion by B. abortus Infected Dendritic Cells.

Brucella infection is characterized by a low induction of proinflammatory and inflammatory mediators, including TNFα, IL1beta, IL-6, IL-10, and IL-12, and LPS is a key molecule in this low recognition by innate immunity (Barquero-Calvo E et al. (2007) PLoS ONE 2: e631). Therefore, it was of interest to study the production of TNFα and IL-12 by BMDCs infected with BAB-parental and with BABΔlpcC and to see if the results were reproduced by stimulation with the LPSs. The results showed the mutant induced a stronger production of both cytokines which was paralleled by the Ba LpcC-LPS ability to stimulate secretion of both cytokines (FIG. 6). Furthermore, experiments in BMDCs obtained from the appropriate TLR mutants demonstrated that the effects were TLR4-dependent and, therefore, directly attributable to the LPS (FIG. 6). In addition, we observed that the minor LPS fraction in the supernatants of the BAB-parental extracts yielded similar results to those obtained with the Ba wt-LPS, but the sediment fraction corresponding to Ba LpcC-LPS failed to stimulate high amounts of either cytokine (not shown).

The LPS Core of B. abortus Modulates Recognition by MD2.

Bacteria carrying a classical LPSs are recognized by the CD-14-MD2 TLR4 system which triggers a cascade of signals leading to cytokine production. In this recognition, MD2 plays a critical role and there is evidence that it interacts with classical LPSs through the core and lipid A section (Gruber A et al. (2004) J Biol Chem 279: 28475-28482; Ohto U et al. (2007) Science 316: 1632-1634). However, it is known that TLR4 mutations do not affect the course of Brucella infections (Barquero-Calvo E et al. (2007) PLoS ONE 2: e631; Lapaque N et al. (2006) Cellular Microbiology 8: 401-413) and that Brucella LPS weakly activates the TLR4-MD2 system (Dueñas A I, et al. (2004) Int Immunol 16: 1467-1475). Since BABΔlpcC induced anomalously high levels of cytokines as compared to BAB-parental, it was of interest to study the interaction of Ba LpcC-LPS with MD2. For this purpose, a competitive ELISA with hMD-2 and an antibody recognizing free hMD2 but not to LPS bound hMD2 was used (Gradisar H et al. (2007) J Leukoc Biol 82: 968-974; Gradisar H et al. (2007) J Leukoc Biol 82: 968-974). In agreement with the low cytokine induction in vivo, Ba wt-LPS did not inhibit antibody binding to hMD2 at any of the concentrations tested. In contrast, Ba LpcC-LPS inhibited binding at 40 μg/mL or higher concentrations, a value that, although clearly different from that of S. enteritidis LPS, departed from that of the Ba wt-LPS (FIG. 7). In this case, the minor fractions of the LPS extracts of both BAB-parental and BABΔlpcC reproduced these results, although not so patently for the latter. These results demonstrate that the LPS core of B. abortus contributes to the low recognition of Brucella LPS by MD2.

Inhibition of Dendritic Cell Maturation by B. abortus Requires and Intact LPS Core.

In response to microbial products, dendritic cells undergo a maturation process that includes the formation of large polyubiquitinated protein aggregates, named dendritic cell aggresome-like induced structures (DALIS). DALIS are thought to contain misfolded proteins and components of the ubiquitin system, suggesting that ubiquitination of misfolded proteins occurs in these structures. It has been suggested that the storage of misfolded self proteins during infection may allow for efficient presentation of peptides from foreign microbial proteins. Brucella interferes with the maturation of dendritic cells, an ability that should favor the establishment of the infection (Salcedo S P et al. (2008) PLoS Pathogens 4: e21). To analyze whether the attenuation of BABΔlpcC in BMDC was accompanied by a defect in this interference, the formation of DALIS was examined using a FK2 Moab which recognizes ubiquitinated proteins (Fujimuro M (1994) FEBS Lett 349: 173-180). As it can be seen in FIG. 8, the BABΔlpcC mutant induced a higher number of DALIS than the parental strain. To relate this effect to the structure of Ba LpcC-LPS, we stimulated BMDC obtained from wild type, TLR4 or TLR9 (as a control) ko mice (data not shown). For the Ba wt-LPS, DALIS were not observed in any kind of dendritic cells. In contrast, Ba LpcC-LPS induced DALIS formation in and TLR9 ko but not in TLR4 ko cells, thereby demonstrating the involvement of the Ba LpcC-LPS in the induction of dendritic cell maturation.

An Intact LPS Core is Required for B. abortus Virulence in Mice.

BABΔlpcC was unable to multiply in BMDCs, suggesting that this mutant could be attenuated in the mouse model. To test this hypothesis, BALBc mice were infected intraperitoneally with the BAB parental and BABΔlpcC and the kinetics of bacterial multiplication in the spleen and the spleen weights compared (FIG. 9). BABΔlpcC showed significant (P=0.0002) attenuation from the 4th week onwards. At the 6th week, the CFU/spleen of BAB-parental were 2 logs higher, and this difference did not change at later times. Splenomegaly increased similarly for both bacteria up to the 4th week. However, whereas spleen enlargement reached a maximum at week 8 for BAB-parental, it began to decrease after week 4 for the BABΔlpcC. In an independent experiment, the spleen CFU of the BABΔlpcC-plpcC complemented strain and the BAB parental strain (mean and standard deviation of log CFU 6.74±0.25 and 6.35±0.31, respectively) were not significantly different (P=0.15) at the time tested (8th week). Moreover, both were significantly different from the CFU obtained for BABΔlpcC in this experiment (4.04±0.49; P<0.001). These results clearly indicated that an intact LPS core is required for full virulence of B. abortus in mice.

Protection in Mice.

Infection in BMDC triggered a strong IL12 response which is anomalous in mouse brucellosis and could result in a protective Thl response. This possibility was consistent with the splenomegaly observed because spleen enlargement correlates with the levels of IFN-γ and IL12 in mouse brucellosis (Zhan Y et al. (1993) Infection and Immunity 61: 4899-4901; Zhan Y et al. (1995) Infection and Immunity 63: 1387-1390) and both cytokines are decisive in generating an effective immunoresponse to Brucella (Baldwin C L et al. (2002) Vet Microbiol 90: 367-382). Interestingly, although animals inoculated with BABΔlpcC would eventually clear the infection (FIG. 11), splenomegaly produced by BABΔlpcC was not only greater than that generated by the BABTn5::per mutant but also consistently higher than that induced by the reference vaccine B. abortus S19 (FIG. 9), For these reasons, we assed the protection against virulent B. abortus induced by vaccination with BABΔlpcC. As it is shown in Table 2, when the spleens were examined 2 weeks after the challenge, BABΔlpcC vaccinated animals contained significantly lower number of CFU/spleen of the challenge strain than the saline control (P<0.001). Moreover, the number of CFU/spleen of the challenge strain were also significantly lower (P=0.025) in the BABΔlpcC vaccinated mice than in the S19 vaccinated ones. The differences between BABΔlpcC and saline vaccinated mice increased six weeks after challenge, and at this time, the immunity afforded by S19 vaccination had completely waned (Table 2).

TABLE 2 Protection against B. abortus infection in BALB/c provided by vaccination with BABΔlpcC or B. abortus S19 X log₁₀ CFU in spleen ± SD of virulent B. abortus at post-challenge week Vaccine 2 6 BABΔlpcC 1.25 ± 0.71^(a,b) 0.81 ± 0.25^(a,c) S19 3.47 ± 1.06^(b) 5.27 ± 0.35^(d) Saline 5.42 ± 0.51 5.49 ± 0.12 ^(a)P versus saline < 0.001. ^(b)P versus S19 < 0.05. ^(c)P versus S19 < 0.001. ^(d)P versus saline > 0.05 (not significant).

Throughout this application, various references describe the state of the art to which this invention pertains. The disclosures of these references are hereby incorporated by reference into the present disclosure. 

1. A method for the treatment of brucellosis, comprising the step of administering to a subject in need thereof a therapeutically effective amount of a gram-negative bacterium carrying an inactivated gene encoding a glycosyltransferase involved in the synthesis of the core of the LPS of said gram-negative bacterium, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having an amino acid sequence of SEQ ID NO:1 or SEQ ID NO: 21 and homologues thereof having an amino acid sequence having at least 50% of identity with SEQ ID NO: 1 or SEQ ID NO: 21, and wherein said inactivated gene encoding a glycosyltransferase involved in the synthesis of the core of the LPS of said Gram-negative bacterium results in the synthesis of a LPS having a modified core.
 2. The method according to claim 1, wherein said amino acid sequence has at least 60% of identity with SEQ ID NO:1 and is selected from the group consisting of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7 and SEQ ID NO:22.
 3. The method according to claim 1, wherein said amino acid sequence has at least 50% of identity with SEQ ID NO:21 and is selected from the group consisting of SEQ ID NO:23, SEQ ID NO:24 and SEQ ID NO:25.
 4. The method according to claim 1, wherein a gene encoding a protein involved in the synthesis of the O-polysaccharide of the LPS is inactivated.
 5. The method according to claim 4, wherein said protein involved in the synthesis of the O-polysaccharide of the LPS is selected from the group consisting of the proteins having the amino acid sequence of SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:26, SEQ ID NO:27 and SEQ ID NO:28 and homologues thereof having an amino acid sequence having at least 50% of identity with an amino acid sequence selected from the group consisting of SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:26, SEQ ID NO:27 and SEQ ID NO:28
 6. The method according to claim 4, wherein said protein involved in the synthesis of the O-polysaccharide of the LPS is a perosamine synthetase having the amino acid sequence of SEQ ID NO:13 or a homologue thereof having an amino acid sequence having at least 90% of identity with the amino acid sequence of SEQ ID NO:13.
 7. The method according to claim 1, wherein said gram-negative bacterium is selected from the group consisting of bacteria of the genus Brucella, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO: 1 or SEQ ID NO: 21, and homologues thereof having an amino acid sequence having at least 60% of identity with NO: 1 or NO: 21, bacteria of the species Ochrobactrum anthropi, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:5, an amino acid sequence having at least 85% of identity with SEQ ID NO:1, the amino acid sequence of SEQ ID NO:23 and an amino acid sequence having at least 62% of identity with SEQ ID NO:21, bacteria of the species Ochrobactrum intermedium, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:6, an amino acid sequence having at least 85% of identity with SEQ ID NO:1, the amino acid sequence of SEQ ID NO:24 and an amino acid sequence having at least 62% of identity with SEQ ID NO:21, bacteria of the species Bartonella henselae, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:22, and an amino acid sequence having at least 69% of identity with SEQ ID NO:1, bacteria of the species Bartonella quintana, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:2 and an amino acid sequence having at least 65% of identity with SEQ ID NO:1, bacteria of the species Bartonella tribocorum, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:3, and an amino acid sequence having at least 64% of identity with SEQ ID NO:1, bacteria of the species Bartonella bacilliformis, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:4, and an amino acid sequence having at least 61% of identity with SEQ ID NO:1, bacteria of the species Agrobacterium tumefaciens, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:7 and an amino acid sequence having at least 63% of identity with SEQ ID NO:1, and bacteria of the species Agrobacterium radiobacter, wherein said glycosyltransferase is selected from the group consisting of the glycosyltransferases having: the amino acid sequence of SEQ ID NO:25 and an amino acid sequence having at least 57% of identity with SEQ ID NO:21.
 8. The method according to claim 7, wherein said bacteria of the genus Brucella is selected from the group consisting of the bacteria of the species Brucella melitensis, Brucella abortus, Brucella suis, Brucella ovis, Brucella pinnipedialis, Brucella ceti, Brucella microti, and Brucella canis. 9-16. (canceled) 